US6263745B1 - Flow cytometer nozzle and flow cytometer sample handling methods - Google Patents

Flow cytometer nozzle and flow cytometer sample handling methods Download PDF

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US6263745B1
US6263745B1 US09/454,488 US45448899A US6263745B1 US 6263745 B1 US6263745 B1 US 6263745B1 US 45448899 A US45448899 A US 45448899A US 6263745 B1 US6263745 B1 US 6263745B1
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flow cytometer
cytometer system
nozzle
sample
exit orifice
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Kris S. Buchanan
Lisa A. Herickhoff
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XY LLC
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Priority to US09/454,488 priority Critical patent/US6263745B1/en
Assigned to XY, INC. reassignment XY, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BUCHANAN, KRIS S., HERICKHOFF, LISA A.
Priority to ES00991511T priority patent/ES2342922T3/es
Priority to PCT/US2000/042350 priority patent/WO2001040765A2/en
Priority to NZ519275A priority patent/NZ519275A/en
Priority to EP10182264.1A priority patent/EP2264430B1/en
Priority to HU0300587A priority patent/HUP0300587A2/hu
Priority to GB0213051A priority patent/GB2372466A/en
Priority to JP2001542181A priority patent/JP5019497B2/ja
Priority to BRPI0016121A priority patent/BRPI0016121B1/pt
Priority to ES10001278.0T priority patent/ES2445520T3/es
Priority to DK00991511.7T priority patent/DK1238261T3/da
Priority to PL00355812A priority patent/PL355812A1/xx
Priority to EP10001278.0A priority patent/EP2180307B1/en
Priority to DK10001278.0T priority patent/DK2180307T3/en
Priority to KR1020077011096A priority patent/KR20070058711A/ko
Priority to BRPI0017624A priority patent/BRPI0017624B1/pt
Priority to CA2393121A priority patent/CA2393121C/en
Priority to MXPA02005488A priority patent/MXPA02005488A/es
Priority to CN00816624A priority patent/CN1402831A/zh
Priority to AU32728/01A priority patent/AU783000B2/en
Priority to AT00991511T priority patent/ATE467113T1/de
Priority to DK10182264.1T priority patent/DK2264430T3/en
Priority to CA2739572A priority patent/CA2739572C/en
Priority to DE60044373T priority patent/DE60044373D1/de
Priority to KR1020027007131A priority patent/KR20020063584A/ko
Priority to RU2002117447/28A priority patent/RU2002117447A/ru
Priority to KR1020077011095A priority patent/KR100909862B1/ko
Priority to EP00991511A priority patent/EP1238261B1/en
Priority to CA2822851A priority patent/CA2822851C/en
Priority to IL14993600A priority patent/IL149936A0/xx
Priority to TW089125453A priority patent/TW538243B/zh
Priority to ARP000106346A priority patent/AR026683A1/es
Priority to UY26469A priority patent/UY26469A1/es
Priority to US09/909,483 priority patent/US6357307B2/en
Application granted granted Critical
Publication of US6263745B1 publication Critical patent/US6263745B1/en
Priority to US10/098,036 priority patent/US6604435B2/en
Priority to NO20022536A priority patent/NO20022536L/no
Priority to ARP020103317A priority patent/AR036412A2/es
Priority to US10/640,337 priority patent/US6782768B2/en
Priority to ARP060102227A priority patent/AR053879A2/es
Priority to ARP060102226A priority patent/AR053878A2/es
Assigned to MERVYN JACOBSON reassignment MERVYN JACOBSON SECURITY AGREEMENT Assignors: XY, INC.
Assigned to XY, INC. reassignment XY, INC. RELEASE OF SECURITY AGREEMENT Assignors: JACOBSON, MERVYN
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Assigned to XY, LLC reassignment XY, LLC CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: XY, INC.
Priority to HK10110051.3A priority patent/HK1143860A1/xx
Priority to JP2011265651A priority patent/JP5762939B2/ja
Assigned to COMPASS BANK, AS ADMINISTRATIVE AGENT reassignment COMPASS BANK, AS ADMINISTRATIVE AGENT SECURITY AGREEMENT Assignors: XY, LLC
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/01—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials specially adapted for biological cells, e.g. blood cells
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G01N15/1409—Handling samples, e.g. injecting samples
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/149—Optical investigation techniques, e.g. flow cytometry specially adapted for sorting particles, e.g. by their size or optical properties
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N2015/1006—Investigating individual particles for cytology
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G01N2015/1413—Hydrodynamic focussing
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G01N2015/1415—Control of particle position
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/10—Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing
    • Y10T436/101666—Particle count or volume standard or control [e.g., platelet count standards, etc.]

Definitions

  • This invention relates to an improved nozzle apparatus for a flow cytometer system and methods for improving flow cytometry. Specifically, this invention relates to a novel design of a nozzle interior surface geometry that gently handles and orients a sample into a proper radial direction for analyzing and efficient sorting. The invention also focuses on systems for sorting delicate cells, especially living sperm cells.
  • a commercially available flow cytometer typically utilizes a cylindrical fluid geometry in its nozzle.
  • This type of flow cytometer system has a focusing flow path with symmetry of revolution, as described in some U.S. patents (U.S. Pat. Nos. 5,602,039, 5,483,469, 4,660,971, 4,988,619 and 5,466,572).
  • This type of design does not produce radially oriented samples.
  • the observed fluorescence intensity depends largely upon the proper orientation of the heads with respect to the detector.
  • Sperm cells emit a stronger fluorescent signal from the edge than the flat surface Therefore, the intensity of the fluorescent signal is dependent on the orientation of the sperm head as it passes the detector.
  • DNA content is determined by fluorescence and because fluorescent intensity is affected by orientation, DNA content determination can be compounded by lack of orientation in a nozzle. For this reason, without radial orientation, the resulting fluorescence intensity distribution obtained for normal, randomly oriented sperm heads reflects both DNA content and head orientation. Because the cells emit a brighter fluorescence signal from the head edge (Gledhill et al., 1976, J. Cell Physiol.
  • certain cells can exhibit decreased functionality as a result of the sort process. This can be particularly true for cells such as mammalian sperm cells which are not only mechanically delicate, but also which can become functionally impaired (as perhaps seen through reduced fertility) or even mortally wounded as a result of some occurrence in the sort process.
  • cells such as mammalian sperm cells which are not only mechanically delicate, but also which can become functionally impaired (as perhaps seen through reduced fertility) or even mortally wounded as a result of some occurrence in the sort process.
  • For flow cytometry efforts with delicate cells there have been significant limitations on abilities. This is most acute in the highly specialized field of sperm cell sorting not only because the cells themselves are unusually delicate, but also because there is a need for extremely high sorting rates for physiological and practical reasons.
  • Hydrodynamic orientation of the sample within the flow cytometer can enhance precise measurement of relative DNA-stain content and can also provide a potentially useful measurement of morphological parameters such as cell thickness and degree of curvature of the flat face. For some applications, this orientation is straightforward. However, when delicate cells (such as sperm cells) or other particles are involved, however, a more gentle technique has been necessary. For example, a sample injection tube with a wedge shaped tip has even been used in some efforts to increase percentage of the oriented cells (Dean et al., 1978, Biophys. J. 23: 1-5; Fulwyler, 1977, J. Histochem. Cytochem.
  • Kachel and his colleagues demonstrated the law of similarity and discussed three types of flow paths that influenced the moving particles. They concluded that, to achieve uniform radial orientation with hydrodynamic forces for flat particles such as flattened red blood cells, the preferred flow path would be the one whereby unilateral constriction can be obtained.
  • the most simple flow path that exhibits an increased unilateral constriction in use with a flow through system would be made of a tube with an ellipsoidal cross section, and would also end in an ellipsoidal outlet.
  • the long axis of this ellipsoidal outlet would be located at a right angle to the long axis in the cross section of the constricting elliptical tube.
  • the elliptical outlet does not produce the type of droplets desired for a high speed flow cytometer cell sorter, this arrangement was not intended to be used in, and has apparently not been applied to, a flow cytometer.
  • Rens and his colleagues designed a nozzle tip that had an elliptical interior and an elliptical exit orifice (Rens et al., 1998, PCT Publication No. PCT/US98/15403; Rens et al., 1998, Cytometry 33: 476-481; Rens et al., 1999, Mol. Reprod. Dev. 52: 50-56).
  • This interior contained a first ellipsoidal zone and a second ellipsoidal zone that were separated by a transitional zone. All the zones each had a long axis and a short axis. The long axis of the second ellipsoidal zone was oriented 90° to that of the first ellipsoidal zone.
  • This device partially solved the problem of random orientation as existed in a conventional flow cytometer and could orient about 60% of the total flattened sperm cells from a boar each time through the flow cytometer. Nevertheless, when hydrodynamic forces in a flow path were taken into consideration, flat particles passing through the nozzle designed by Rens and his colleagues have received unnecessary stresses. For delicate cells, and especially for the perhaps more delicate sperm cells such as equine or bovine sperm cells, this approach simply did not appear to yield the desired efficiency either in orientation or in cell viability.
  • This improved nozzle interior surface geometry can comprise either or both of: an appropriately configured accelerative force feature and/or an elliptical-like, single torsional interior surface element within a single torsional orientation nozzle that produces the special hydrodynamic forces, namely, single torsional orientation forces.
  • the problems with undesirable cell stress could be viewed as at least in part due to either inappropriate handling forces, specifically: inappropriate accelerative forces, or the existence of a second torsional force created by the second ellipsoidal zone.
  • the accelerative forces applied devices often utilized abrupt transitions internal to the nozzle and so caused extreme acceleration over short distances.
  • approaches such as that of Ren (mentioned earlier) showed, that after cells had been oriented by a first torsional force created by a first ellipsoidal zone, an additional—perhaps doubling—stress was applied.
  • the flat particles were already in an oriented position after they were oriented from a random position by the first ellipsoidal zone.
  • Yet another object is to present a system which can more quickly and more accurately measure and sort the sample, especially delicate sperm cells in research and clinical use and in the animal insemination industry.
  • a further object to provide methods for improving orientation and sorting efficiency of the sample, especially the sperm cells in the flow cytometry for research and clinical use and animal insemination industry.
  • FIG. 1 is a cross sectional view of a portion of a flow cytometer showing a sheath fluid container, a sample injection tube and a nozzle of the present invention. This figure also shows a relative location of the sample tube within the nozzle.
  • FIG. 2 is a three-dimensional view of one nozzle tip and its relative position with the sheath fluid container (here the nozzle body) with a sample injection tube and a nozzle tip.
  • FIG. 2A is a schematic drawing of the sample injection tube that has a beveled tip and a circular mouth.
  • FIGS. 3A, 3 B, and 3 C are schematic drawings of one of the present embodiments of the nozzle.
  • FIG. 3A is a three-dimensional view of the nozzle tip showing the first ellipticity-increasing zone, the desired ellipse demarcation location, the ellipticity-decreasing zone, the conical zone, the cylindrical zone, and the circular exit orifice.
  • FIG. 3B is a schematic cross sectional view showing the tapered interior surface of the nozzle in a unitary design.
  • FIG. 3C is a cross sectional view of the cylindrical zone and the circular exit orifice.
  • FIG. 4A is a bottom view of the nozzle tip region showing specifically the circular exit orifice.
  • FIG. 4B is a top view of the interior design of the nozzle showing the largest circular mouth, the desired ellipse demarcation location, the larger circular mouth of the conical zone and the smallest circular mouth of the cylindrical zone.
  • the diameter of the smallest mouth is also that of the circular exit orifice.
  • FIG. 5 shows how the single torsional orientation nozzle works in orienting flat particles.
  • FIG. 6 is a schematic diagram of an example of a nozzle having axial motion surfaces as may have existed in the prior art.
  • FIGS. 7 a , 7 b , and 7 c are plots of the theoretical axial velocity, acceleration, and rate of change of acceleration motions with respect to location as may exist for a nozzle such as that shown schematically in FIG. 6 .
  • FIG. 8 is a schematic diagram of an example of a nozzle having axial motion surfaces according to one embodiment of the present invention.
  • FIGS. 9 a , 9 b , and 9 c are plots of the theoretical axial velocity, acceleration, and rate of change of acceleration motions with respect to location as may exist for a nozzle such as that shown schematically in FIG. 8 .
  • FIG. 1 shows a portion of a flow cytometer system where a sample is processed into individual droplets prior to being analyzed and sorted.
  • a sheath fluid container ( 1 ) may contain some sheath fluid ( 2 ) imported through a sheath fluid port (not shown).
  • a sample injection system comprises a sample injection tube ( 3 ) connected to a sample reservoir (not shown). The sample injection system generally acts to provide the appropriate flow of some sample material to a nozzle system.
  • the sheath fluid container at the same time introduces a sheath fluid into the nozzle system.
  • the sample may be surrounded by the sheath fluid to form a sample-containing fluid and may then exit the nozzle system through a drop-forming mechanism through which the sample-containing fluid forms small droplets.
  • These small droplets may pass through a free falling area at a high speed of over about 20 meters per second by combination of oscillation by an oscillator and high pressure from the flow cytometer system. Subsequently, these small droplets, i.e., the sample-containing drops, may be analyzed by an analytical system (not shown) at the free falling area. If living cells such as flat sperm cells are introduced as the sample material, they may be stained with one or more fluorescent dyes.
  • sperm cells may be carried in single file in the sheath fluid stream past the analytical system (not shown).
  • the analytical system may include a focused laser whose wavelength is adjusted to excite a fluorescent dye that may be present.
  • the fluorescence signal collected from each cell can then be sensed through a detecting system (not shown).
  • this process may include a sorting process by a sorting device or the like, depending on the individual physical property such as the DNA content of each cell introduced, through the differential application of charge to the various droplets as those skilled in the art readily understand. Subsequently, each cell is sorted depending on its charge.
  • these general aspects of flow cytometry are well known and are discussed in the references mentioned earlier (hereby incorporated by reference).
  • torsional alignment In relation to the handling of the sample for the flow cytometer's functions and the sample's viability, two aspects can be important: torsional alignment and the sample's axial motion. Each of these is discussed separately, however, it should be understood that they are not mutually exclusive and can synergistically have effects. This is especially true as it relates to the sample's viability, that is, the ability of the sample to perform its functions with efficacies expected and not substantially affected by the flow cytometry processing. The first of these two aspects, torsional alignment, is discussed first.
  • FIG. 1 The aspects illustrated in FIG. 1 can also be seen through the three-dimensional view shown in FIG. 2 .
  • This three dimensional view shows a portion of the flow sheath container ( 2 ), the sample injection tube ( 3 ) and the nozzle system having a nozzle ( 6 ).
  • the sample injection tube ( 3 ) as shown in FIG. 2A in detail, has a beveled tip ( 4 ) and a circular mouth ( 5 ).
  • the specially designed nozzle ( 6 ) is termed a single torsional orientation nozzle in the present invention and will be presented in detail below.
  • the sample injection tube serves to introduce the sample material in thin flow into the nozzle system where the sample is surrounded by the sheath fluid.
  • the conventional sample injection tube often has a cylindrical shape.
  • this type of sample injection tube may not help in controlling orientation of the sample, the sample coming out from this type of the sample injection tube usually has a non-oriented status.
  • a modified sample injection tube was produced (Dean et al., 1978, supra; Fulwyler, 1977, supra; Johnson et al., 1986, Cytometry 7: 268-273; Pinkel et al., 1982, supra).
  • This modified sample injection tube may have a beveled tip and can help, to some degree, in orienting the sample material coming out of its tip. Because of the beveled shape at the tip of the sample injection tube, the sample stream can be drawn into a thin ribbon by the sheath fluid. The resulting change in flow condition can cause a corresponding orientation of the sample material.
  • the sample injection tube ( 3 ) termed here an orientation-improving sample injection tube, comprises a beveled tip ( 4 ) and a circular mouth ( 5 ) in its cross section.
  • the beveled tip is more or less a rectangular shape in its cross section. This has a long axis and a short axis. While naturally this may be varied to suit the application or the particles being sorted, in one preferred embodiment the angle of the beveled tip is about 4°, the outer diameter of the tube is about 1.5 mm and the diameter of the circular mouth is about 0.25 mm.
  • the flow cytometer system comprises the uniquely designed single torsional orientation nozzle ( 6 ).
  • the single torsional orientation nozzle ( 6 ) may be made of some selective Is materials such as a ceramic material and the like.
  • the size of the nozzle e.g., the height and the diameter, etc., may be varied, it should preferably fit into a conventional flow cytometer and at the same time provide the desired orientation forces as described in this present invention.
  • the nozzle is made into a single piece, for the purpose of a better illustration, it may be divided into two portions, i.e., an upper cylindrical portion (a) and a lower conical portion (b).
  • the height of the upper cylindrical portion (a) may be about 8 mm and the outer diameter may be about 6 mm.
  • the height of the conical portion (b) may be about 4.5 mm and the outer diam at the orifice may be less than about 1 mm.
  • the total height of the nozzle may be about 12.5 mm.
  • the use of a unitary nozzle also aids in fixing all orientation and axial motion factors in an optimum arrangement. It can thus increase ease of use, repeatability, and other practical matters as well.
  • FIG. 3A is a three-dimensional view and FIGS. 3B & 3C are schematic cross sectional views of a single torsional orientation nozzle of the present invention.
  • the single torsional orientation nozzle ( 6 ) comprises a nozzle volume enclosed by an interior surface element.
  • the interior surface element of the single torsional orientation nozzle constitutes its interior geometry.
  • the interior surface element may comprise a single torsional interior surface element having a single torsional interior surface. This single torsional interior surface element has the ability of generating single torsional hydrodynamic forces having a hydrodynamic axis when a flow containing the sample passes through it.
  • the single torsional interior surface element also has a velocity accelerating characteristic that may produce an accelerating velocity upon the sample.
  • the sample may be oriented by the single torsional hydrodynamic forces and radially aligned with respect to the hydrodynamic axis. It may also be accelerated to exit for the subsequent analysis and sorting process.
  • These special single torsional hydrodynamic forces may be referred to as single torsional orientation forces.
  • the overall shape of the single torsional interior surface is gradually tapered downstream so it may be referred as a gradually tapered, single torsional interior surface element.
  • this gradually tapered, single torsional interior surface element may be viewed in two dimension as being a “fan-like” shape that opens from the bottom to the top.
  • the tapered degree of the gradually tapered, single torsional interior surface element may vary but may preferably be about 23° from the bottom of the “fan-like” shape to the top so that the desired accelerating force may be generated to act upon the sample.
  • the gradually tapered, single torsional interior surface element may be divided into a few zones based upon its interior geometry and each zone may have a laminar flow surface.
  • the gradually tapered, single torsional interior surface element may be made of a tapered, elliptical-like interior zone (c) having an elliptical-like, single torsional interior surface and a cylindrical interior zone (d) in the three-dimensional view.
  • This elliptical-like, single torsional interior surface may include different shapes in its cross sections. For example, besides being ellipse-shaped, it may be oval-shaped, or even close to a rectangle-shape. Any of these shapes may occur at any location along the elliptical-like, single torsional interior surface just above and below a demarcation location at which its ellipticity, ovality, or even rectangularity reaches a maximum or desired degree.
  • each of these shapes is intended to be encompassed by the term “elliptical-like” even though a true mathematical ellipse is not present at a given cross section.
  • the term “circular” need not be perfectly circular—or even circular at all. Again, it may be preferred to be circular, however, other shapes may be equivalent so long as the appropriate function is present.
  • the tapered, elliptical-like interior zone may have a major axis and a minor axis in its cross sections and the ellipticity may be smoothly controlled.
  • this tapered, elliptical-like interior zone may be divided into the following zones from the top downstream to the bottom:
  • the two dimensional shapes of the cross sectional view from the top to the bottom of the tapered, elliptical-like interior zone may undergo transitional changes from a circle at the mouth region, to elliptical-like shapes (which may even be actual ellipses) with gradually increasing ellipticity (that is the ratio of major to minor axes—regardless of the shape involved), to the desired ellipse or the like, to elliptical-like shapes with gradually decreasing ellipticity, and finally to a circle again at the region where the tapered elliptical-like interior zone joins the cylindrical zone.
  • the ellipticity may thus be adjusted by changing the ratio of the major to the minor axis.
  • the major to the minor axis ratio may gradually change from the top from 1 to larger than 1, or perhaps even an optimal ratio for the sample.
  • the optimal ratio may be a maximum ratio.
  • the ratio may gradually change back from the maximum ratio to smaller than the maximum ratio and then to 1.
  • the ratio becomes 1 the shape in cross section may be a circle.
  • the maximum ratio as referred above may vary to some degree.
  • the length of the major axis may be 2.2 mm and that of the minor axis may be 1.0 mm.
  • the maximum ratio is designed to be about 2.2 for this one preferred embodiment. Naturally it may vary based on application or the like.
  • the desired ellipse demarcation location ( 9 ) downstream the ellipticity-increasing zone ( 8 ) within the nozzle may be the place where the beveled tip of the sample injection tube is located. This may also be the place where the sample in the ribbon flow receives desired orientation forces that are fully functional, where the sample is minimally torqued by the desired orientation forces or torquing forces, where the time required for cell to exit is minimal, or where the sample after exiting from the orifice of the nozzle can still well maintain its oriented status so the subsequent analysis and sorting can be conducted efficiently.
  • This location may be referred as an injection point.
  • this location or the injection point may be about 6 mm from the exit orifice.
  • an orientation maintaining distance is defined as the distance that indicates how far a sample particle can maintain its oriented status from the point at which it is oriented to a point at which it statistically loses its degree of oriented status
  • the distance from the beveled tip of the sample injection tube to the exit orifice of the nozzle and the distance from the exit orifice to the intersection with the laser beam or sensor along the flow path in the falling zone well falls within this orientation maintaining distance.
  • any sample particles that are oriented, no matter at which point within the distance from the beveled tip to the intersection with the laser beam or sensor, will maintain their oriented status before they are analyzed.
  • this orientation maintaining distance could even be longer than 10 mm when a flow cytometer is equipped with the specially designed nozzle of the present invention and the sample injection tube with the beveled tip.
  • the long axis of the beveled tip may be aligned with the major axis of the desired ellipse demarcation location and short axis is with the minor axis as shown.
  • elliptical-like interior zone (c) may be a cylindrical interior zone (d).
  • This cylindrical interior zone (d), as can be seen in both FIGS. 3A, 3 B, and 3 C may be further divided into a conical zone ( 12 ) that is tapered and a cylindrical zone ( 14 ).
  • the conical zone ( 12 ) has a larger circular mouth ( 11 ) at the top that joins with the tapered elliptical-like interior zone (c) and a smaller circular orifice ( 13 ) in connection with the cylindrical zone ( 14 ).
  • the larger circular mouth ( 11 ) at the top of the conical zone may be about 0.19 mm in diameter and the circular opening may be about 0.07 mm in one preferred embodiment.
  • the height of the conical zone may be about 0.3 mm.
  • the cylindrical zone ( 14 ) may also have a mouth with the same diameter as the smaller opening of the conical zone throughout its circular exit orifice ( 15 ) and may be about 0.15 mm in height.
  • FIG. 4A illustrates a bottom view of the single torsional orientation nozzle showing the circular orifice.
  • the circular orifice should be small enough so that tiny droplets containing sample particles may be formed.
  • the diameter in one of the preferred embodiments may be about 0.07 mm.
  • FIG. 4B shows a top view of the single torsional orientation nozzle. As can be seen clearly, the mouth may be in a circular shape with a diameter of about 5.25 mm.
  • FIG. 5 it can be seen how orientation occurs.
  • this figure is a modified drawing from Kachel and his colleagues (FIG. 3, Kachel et al., 1977, J. Histochem. Cytochem. 25: 774-780).
  • This drawing a cross section around the desired demarcation ellipse location ( 9 ), shows, first of all, the distributions of the orientation forces generated from the elliptical-like, single torsional interior surface.
  • the dissimilar transformation of the elliptical-like, single torsional interior surface can cause preferential side forces to generate additional flow components along the major axis and may decrease the forces generated along the minor axis.
  • the forces generated along the major axis may be viewed as stronger than the forces generated along the minor axis to thus orient a flat particle ( 16 ) as shown.
  • the unique design of the present invention shows its superiority in that the tapered, elliptical-like interior zone (c) is connected directly to the cylindrical interior zone (d) and the circular exit orifice ( 15 ).
  • This specially designed geometry successfully avoids the law of similarity and, therefore, the sample particles that have been oriented will be able to individually exit the circular exit orifice and still maintain their orientationally aligned status.
  • the whole tapered, single torsional interior surface element may be viewed to comprise a laminar flow surface.
  • the sample may be radially oriented and aligned along the hydrodynamic axis.
  • the orientationally aligned sample is thus maintained at the orientationally aligned status when exiting the circular exiting orifice where the sample is split into individual particles and the like, is surrounded by a sheath fluid drop, and is analyzed. Therefore, the finally oriented sample can be due to the combined efforts from the beveled tip of the sample injection tube and the single torsional orientation interior surface that, because of the unique geometry, generates single torsional orientation forces and produces laminar flow.
  • the whole interior surface of the single torsional orientation nozzle may be unitary.
  • the way of dividing the whole interior surface into the tapered, elliptical-like interior zone (c) the cylindrical interior zone (d) and their own subsequent zones as described above is purely for a clear explanation purpose.
  • the buffered sperm cells may be injected at the demarcation location within the elliptical-like, single torsional interior surface element of the single torsional orientation nozzle where they may be surrounded by the sheath fluid to form a sheath-surrounded sperm.
  • the sperm-containing drops may be produced by a drop-forming mechanism and analyzed at the free falling area.
  • the sperm-containing drops are then charged and sorted by the sorting device and colleted by a sperm-compatible collecting system containing a specially made sperm-collecting fluid. This whole process may minimize the stresses upon the sperm created through the sorting process.
  • the X or Y-chromosome-bearing sperm may then be used for insemination and production of a mammal of a desired sex.
  • this single torsional orientation nozzle when specially combined with the beveled sample injection tube located at an appropriate location relative to a specific region of the interior surface of the single torsional orientation nozzle, can provide results which may be even more satisfactory.
  • a second important aspect is that of the sample's axial motion. This aspect encompasses not only the motion of the sample as it traverses the nozzle down the central axis, but the stresses the sample receives during its path. These motions can perhaps be most easily characterized by three values, the three derivatives of distance with respect to location along the sample. These derivatives can be summarized by the following:
  • the nozzle may present any number of axial motion surfaces, that is surfaces which influence or perhaps only confine the sample as it passes through the nozzle.
  • the axial motion surfaces may be symmetric pairs and may also be as simple as a first axial motion surface ( 21 ) and a second axial motion surface ( 22 ).
  • these axial motion surfaces can act in manners which influence the sample or its viability.
  • the sample is thus (usually hydrodynamically) subjected to a first axial motion surface ( 21 ). It may then transition at a transition location ( 23 ) to become influenced by a second axial motion surface ( 22 ). After the transition location ( 23 ) the sample is then subjected to the second axial motion surface ( 22 ). It may then exit the nozzle such as at the circular exit orifice ( 15 ).
  • the axial motion surfaces can have any shape. In a system, such as one that may have constant velocity, they may have a tubular shape. As shown in FIGS. 6 & 8, in a system such as one that achieves acceleration of the sample as it passes through the nozzle ( 6 ), they may be configured as acceleration surfaces such as the conical surfaces shown. The acceleration surface could also decelerate the sample, of course. By causing acceleration or deceleration, the surface would at so as to change the velocity of the sample as it passes through the nozzle ( 6 ). Thus, it can be understood that the nozzle ( 6 ), such as shown in FIG. 8 may include a first axial acceleration surface ( 24 ) and a second axial acceleration surface ( 25 ).
  • the first axial acceleration surface ( 24 ) causes the sample to experience an a first acceleration value (which may or may not be constant) and the second axial acceleration surface ( 25 ) can cause the sample to experience a second acceleration value.
  • This second acceleration value may or may not be different from the first. As shown in FIG. 8, since the second acceleration surface ( 25 ) converges at a different rate, it likely would indicate a different acceleration value.
  • the sample may experience a stress.
  • This stress can have impacts on the samples viability and functionality.
  • One particular aspect for some samples, such as longer cells, may be the fact that when there is a change in velocity, there may be differences in the velocity tendency from one end of the sample to the next. This may be most easily understood in reference to a sample such as a sperm cell.
  • Viable sperm cells have heads and tails. When the head is accelerated differentially from the acceleration of the tail, or when the head is moved at a velocity different from that of the tail, a differential may be created from head to tail. This differential may cause stress on the cell. In extreme cases, it may even pull the tail from the head. Obviously this could destroy the efficacy of the sample.
  • the present invention provides a system through which this can be minimized and the undesirable effects can be avoided or reduced. This is accomplished by subjecting the sample to a “low” degree of changes in acceleration or velocity across the sample's length.
  • “low” may be a relative term which can depend on the cell and the environment. It may be theoretically or empirically determine as a value which is shown to achieve practical percentages of efficacy in the sample for its specific application. These probabilities may be such as at least 70%, 80%, 90%, or the like.
  • the “low” acceleration or rate of change in acceleration may also be affirmatively applied.
  • Changes in acceleration or velocity can occur when the axial motion surfaces change. These changes can be abrupt or gentle. Naturally some embodiments of the present invention prefer the latter. Referring to FIG. 6, it can be seen how an abrupt change in the axial motion surface along the axis can stress the sample.
  • the first axial motion surface ( 21 ) changes in a discrete fashion at the transition location ( 23 ).
  • the second axial motion surface ( 22 ) is created by a separate element, such as by the insertion of a jewel, there can exist a discontinuity in the nozzle ( 6 ). At such a point, the sample can then be subjected to an extreme change in velocity almost instantaneously. Note that such a discrete change may exist unintentionally, due to almost imperceptible misalignments.
  • the present invention can avoid or minimize the stresses thus created.
  • the transition can be a continuous transition as in curved area, by having a limited amount of ‘discreteness’ or misalignment, or may just avoid the possibility of a discrete change by having an inner surface on the nozzle ( 6 ) which is unitary. In this manner, the nozzle may effectively have a unitary surface.
  • the nozzle ( 6 ) can be affirmatively designed so as to present a transition with a maximal acceleration differentiation. As shown in FIG. 8, this may be done through designing in a limited maximal acceleration differentiation transition area ( 26 ) such as shown between the first axial motion surface and the second. It may also be accomplished by using a unitary exit orifice. The limited maximal acceleration differentiation transition area can then be at or as a result of the unitary exit orifice.
  • FIGS. 7 a-c and 9 a-c are graphical representations of the three derivative values at respective locations in their adjacent nozzles shown in FIGS. 6 & 8.
  • FIGS. 7 a and 9 a represent the first derivative of distance with respect to location, a concept similar to velocity. Since the nozzle in FIG. 6 has a discrete change at the transition location ( 23 ), it can be seen that dl/dl changes discretely at the transition location ( 23 ). For the nozzle ( 6 ) in FIG. 8, the dl/dl value does not discretely change. This the sample may be treated to less stress for this reasons alone.
  • FIGS. 7 a-c and 9 a-c are graphical representations of the three derivative values at respective locations in their adjacent nozzles shown in FIGS. 6 & 8.
  • FIGS. 7 a and 9 a represent the first derivative of distance with respect to location, a concept similar to velocity. Since the nozzle in FIG. 6 has a discrete change at the transition location ( 23 ),
  • the d 2 l/dl 2 values for their respective nozzle are also different.
  • the second derivative of distance with respect to location value (or perhaps more easily viewed as acceleration) has a moment of extreme change. Again, this is not so present in FIG. 9 b .
  • the third derivative of distance with respect to location values, d 3 l/dl 3 (or perhaps more easily viewed as rate of change of acceleration) also differ.
  • the value first goes positive and then negative. In the values shown in FIG. 9 c , the values never change signs, they are either zero or positive, but never negative.
  • An other aspect which may be a factor for some samples is the aspect of the duration of the velocity, acceleration, or rate of change of acceleration as experienced by the sample. This may also be referred to as the dwell time for the sample.
  • the dwell time for the sample In flow cytometry, there is often a need for single samples to be placed in single drops. Aspects such as this can cause a desire to transition the fluid at the last possible time. In systems which attempt to do this, it can be important to pay particular attention to areas in the vicinity is about 100 um of the exit point ( 27 ), areas more than 300 um away from the exit point ( 27 ), areas in the vicinity of the exit point ( 27 ), or even areas away from the exit point ( 27 ). In addition, in some systems it may be acceptable to only momentarily subject the sample to the undesired values. Thus limits can be established throughout the nozzle ( 6 ) or at specific locations within the nozzle ( 6 ). Some of the limits which can be applied are set forth in table s 1 & 2.
  • the values may also be established over the effective cell/sample length. These lengths can be both theoretically determined, measured as the actual sample length, or even be empirically determined as an effective sample length. Again, these affirmative or coordinated actions result in avoiding leaving things to chance and can permit certainty for users. In the empirical determinations, among others, it should be understood that the values achieved may be chosen so as to not exceed the practical capabilities of the sample over its length, that is so that the sample retain a sufficiently acceptable probability of functionality after they are processed. In these manners, by coordinating the maximal acceleration differentiation, by affirmatively limiting the maximal acceleration differentiation, and by affirmatively choosing values (determined or not) so as to not exceed the practical capabilities of the sample, the present invention can achieve its ends.
  • sperm cells sperm collection systems, bovine sperm cells, equine sperm cells, sperm cells which have been stained and sorted by their DNA content (such as in sexed sperm cells), sorted male or female bovine sperm cells, and even sorted male or female equine sperm cells.
  • the basic concepts of the present invention may be embodied in a variety of ways. It involves both exercise techniques as well as devices to accomplish the appropriate exercise.
  • the exercise techniques are disclosed as part of the results shown to be achieved by the various devices described and as steps which are inherent to utilization. They are simply the natural result of utilizing the devices as intended and described.
  • some devices are disclosed, it should be understood that these not only accomplish certain methods but also can be varied in a number of ways. Importantly, as to all of the foregoing, all of these facets should be understood to be encompassed by this disclosure.
  • each of the various elements of the invention and claims may also be achieved in a variety of manners.
  • This disclosure should be understood to encompass each such variation, be it a variation of an embodiment of any apparatus embodiment, a method or process embodiment, or even merely a variation of any element of these.
  • the words for each element may be expressed by equivalent apparatus terms or method terms—even if only the function or result is the same.
  • Such equivalent, broader, or even more generic terms should be considered to be encompassed in the description of each element or action. Such terms can be substituted where desired to make explicit the implicitly broad coverage to which this invention is entitled.

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US09/454,488 1999-12-03 1999-12-03 Flow cytometer nozzle and flow cytometer sample handling methods Expired - Lifetime US6263745B1 (en)

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US09/454,488 US6263745B1 (en) 1999-12-03 1999-12-03 Flow cytometer nozzle and flow cytometer sample handling methods
EP00991511A EP1238261B1 (en) 1999-12-03 2000-11-29 Flow cytometer sample handling method
CA2822851A CA2822851C (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
IL14993600A IL149936A0 (en) 1999-12-03 2000-11-29 Flow cytometer nozzle and flow cytometer sample handling methods
RU2002117447/28A RU2002117447A (ru) 1999-12-03 2000-11-29 Насадок проточного цитометра и способы обработки проб посредством проточного цитометра
KR1020027007131A KR20020063584A (ko) 1999-12-03 2000-11-29 개선된 플로우 사이토미터 노즐 및 플로우 사이토미터샘플 처리 방법
CA2393121A CA2393121C (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
CA2739572A CA2739572C (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
KR1020077011095A KR100909862B1 (ko) 1999-12-03 2000-11-29 개선된 플로우 사이토미터 노즐 및 플로우 사이토미터 샘플처리 방법
NZ519275A NZ519275A (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
EP10182264.1A EP2264430B1 (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
HU0300587A HUP0300587A2 (hu) 1999-12-03 2000-11-29 Áramlási citometriás mintafeldolgozási eljárás, eljárás szexált hímivarsejtminta, valamint emlős előállítására
GB0213051A GB2372466A (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
JP2001542181A JP5019497B2 (ja) 1999-12-03 2000-11-29 改良されたフローサイトメーターノズルおよびフローサイトメーターのサンプル操作方法
BRPI0016121A BRPI0016121B1 (pt) 1999-12-03 2000-11-29 dispositivo para citômetro de fluxo, com bocal
ES10001278.0T ES2445520T3 (es) 1999-12-03 2000-11-29 Boquilla de citómetro de flujo
DK00991511.7T DK1238261T3 (da) 1999-12-03 2000-11-29 Fremgangsmåde til behandling af en flowcytometerprøve
PL00355812A PL355812A1 (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
EP10001278.0A EP2180307B1 (en) 1999-12-03 2000-11-29 Flow cytometer nozzle
DK10001278.0T DK2180307T3 (en) 1999-12-03 2000-11-29 Flow cytometry nozzle
KR1020077011096A KR20070058711A (ko) 1999-12-03 2000-11-29 개선된 플로우 사이토미터 노즐 및 플로우 사이토미터 샘플처리 방법
BRPI0017624A BRPI0017624B1 (pt) 1999-12-03 2000-11-29 método de processamento de amostra para citômetro de fluxo
PCT/US2000/042350 WO2001040765A2 (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
MXPA02005488A MXPA02005488A (es) 1999-12-03 2000-11-29 Boquilla mejorada para citometro de flujo y metodos para el manejo de muestra de citometro de flujo.
CN00816624A CN1402831A (zh) 1999-12-03 2000-11-29 改进的流式血细胞计数器喷嘴和流式血细胞计数器样品的处理方法
AU32728/01A AU783000B2 (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample handling methods
AT00991511T ATE467113T1 (de) 1999-12-03 2000-11-29 Durchflusszytometerprobenbehandlungsverfahren
DK10182264.1T DK2264430T3 (en) 1999-12-03 2000-11-29 Improved flow cytometer nozzle and flow cytometer sample processing methods
ES00991511T ES2342922T3 (es) 1999-12-03 2000-11-29 Procedimiento de manipulacion de muestras de un citometro de flujo.
DE60044373T DE60044373D1 (de) 1999-12-03 2000-11-29 Durchflusszytometerprobenbehandlungsverfahren
TW089125453A TW538243B (en) 1999-12-03 2000-11-30 Improved flow cytometer nozzle and flow cytometer sample handling methods
ARP000106346A AR026683A1 (es) 1999-12-03 2000-12-01 Boquilla mejorada para citometro de flujo y metodos para el manejo de muestra de citometro de flujo
UY26469A UY26469A1 (es) 1999-12-03 2000-12-04 Boquilla mejorada para citómetro de flujo y métodos para el manejo de muestra de citómetro de flujo
US09/909,483 US6357307B2 (en) 1999-12-03 2001-07-20 System and method of flow cytometry and sample handling
US10/098,036 US6604435B2 (en) 1999-12-03 2002-03-13 Low acceleration method of flow cytometry
NO20022536A NO20022536L (no) 1999-12-03 2002-05-28 Forbedret munnstykke for strömningscytometer og fremgangsmåter for håndtering av pröver fra strömningscytometer
ARP020103317A AR036412A2 (es) 1999-12-03 2002-09-02 Un metodo de procesamiento de muestra de citometria de flujo, un metodo de crear un especimen de esperma sexuado y un metodo para crear un mamifero
US10/640,337 US6782768B2 (en) 1999-12-03 2003-08-12 Flow cytometer nozzle
ARP060102227A AR053879A2 (es) 1999-12-03 2006-05-29 Un metodo de procesamiento de muestra de citometria de flujo , un metodo de crear un especimen de esperma sexuado y un metodo para crear un mamifero
ARP060102226A AR053878A2 (es) 1999-12-03 2006-05-29 Una disposicion de citometro de flujo, un especimen de esperma sexuado y un mamifero
HK10110051.3A HK1143860A1 (en) 1999-12-03 2010-10-25 Flow cytometer nozzle
JP2011265651A JP5762939B2 (ja) 1999-12-03 2011-12-05 改良されたフローサイトメーターノズルおよびフローサイトメーターのサンプル操作方法

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US10/098,036 Expired - Lifetime US6604435B2 (en) 1999-12-03 2002-03-13 Low acceleration method of flow cytometry
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Cited By (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6357307B2 (en) 1999-12-03 2002-03-19 Xy, Inc. System and method of flow cytometry and sample handling
WO2002092247A1 (en) * 2001-05-17 2002-11-21 Cytomation, Inc. Flow cytometer with active automated optical alignment system
US20040050064A1 (en) * 2002-06-21 2004-03-18 Darko Segota Method and system for regulating internal fluid flow within an enclosed or semi-enclosed environment
US20040062685A1 (en) * 2002-09-27 2004-04-01 Norton Pierce O Fixed mounted sorting cuvette with user replaceable nozzle
US20040104309A1 (en) * 2002-06-21 2004-06-03 Darko Segota Method and system for regulating external fluid flow over an object's surface, and particularly a wing and diffuser
US20040132001A1 (en) * 2000-11-29 2004-07-08 Seidel George E System for in-vitro fertilization with spermatozoa separated into x-chromosome and y-chromosome bearing populations
WO2004088283A2 (en) * 2003-03-28 2004-10-14 Monsanto Technology Llc Apparatus and methods for providing sex-sorted animal sperm
US20050003472A1 (en) * 2003-03-28 2005-01-06 Monsanto Technology Llc Process for the staining of sperm
US6861265B1 (en) * 1994-10-14 2005-03-01 University Of Washington Flow cytometer droplet formation system
US20050072677A1 (en) * 2003-02-18 2005-04-07 Board Of Regents, The University Of Texas System Dielectric particle focusing
US20050098685A1 (en) * 2002-06-21 2005-05-12 Darko Segota Method and system for regulating pressure and optimizing fluid flow about a fuselage similar body
US20050106016A1 (en) * 2002-06-21 2005-05-19 Darko Segota Method and system for regulating fluid flow over an airfoil or a hydrofoil
US20050214733A1 (en) * 2004-03-29 2005-09-29 Monsanto Technology Llc Sperm suspensions for use in insemination
US20050282245A1 (en) * 2004-03-29 2005-12-22 Monsanto Technology Llc Use of a composition which regulates oxidation/reduction reactions intracellularly and/or extracellularly in a staining or sorting process
US20080153087A1 (en) * 2004-02-05 2008-06-26 Select Xy Limited Method and Apparatus For Orienting Aspherical Cells
US20090283148A1 (en) * 2008-05-13 2009-11-19 Sony Corporation Microchip and channel structure for the same
US20100009333A1 (en) * 2008-07-08 2010-01-14 Beckman Coulter, Inc. Methods for Acoustic Particle Focusing in Biological Sample Analyzers
DE102008033570A1 (de) * 2008-07-15 2010-02-11 Masterrind Gmbh Verfahren zur Zellidentifikation und Zellsortierung
US7713687B2 (en) 2000-11-29 2010-05-11 Xy, Inc. System to separate frozen-thawed spermatozoa into x-chromosome bearing and y-chromosome bearing populations
US7723116B2 (en) 2003-05-15 2010-05-25 Xy, Inc. Apparatus, methods and processes for sorting particles and for providing sex-sorted animal sperm
US7772005B1 (en) 1998-07-30 2010-08-10 Xy, Llc Method of establishing an equine artificial insemination sample
US7820425B2 (en) 1999-11-24 2010-10-26 Xy, Llc Method of cryopreserving selected sperm cells
US7833147B2 (en) 2004-07-22 2010-11-16 Inguran, LLC. Process for enriching a population of sperm cells
US7855078B2 (en) 2002-08-15 2010-12-21 Xy, Llc High resolution flow cytometer
US20110071035A1 (en) * 1997-01-31 2011-03-24 Xy, Llc Optical Apparatus
US20110236923A1 (en) * 2010-03-23 2011-09-29 Genetics & Ivf Institute Method for staining and sorting of a small volume of sperm
US8211629B2 (en) 2002-08-01 2012-07-03 Xy, Llc Low pressure sperm cell separation system
WO2012106294A1 (en) 2011-02-04 2012-08-09 Cytonome/St, Llc Particle sorting apparatus and method
AU2012200711B2 (en) * 2003-03-28 2012-09-20 Inguran, Llc "Method and apparatus for orientating sperm in a fluid stream"
US20130020498A1 (en) * 2011-07-19 2013-01-24 Sysmex Corporation Flow cytometer
US8486618B2 (en) 2002-08-01 2013-07-16 Xy, Llc Heterogeneous inseminate system
WO2014047358A1 (en) 2012-09-19 2014-03-27 Inguran, Llc Flow cytometer nozzle tip
WO2014046733A1 (en) 2012-09-19 2014-03-27 Inguran, Llc Nozzle assembly for a flow cytometer system and methods of manufacture
WO2014055112A1 (en) 2012-10-05 2014-04-10 Inguran, Llc High efficiency methods of sex sorting sperm
US20140261757A1 (en) * 2013-03-13 2014-09-18 Sony Corporation Flow channel device, particle sorting apparatus, particle outflow method, and particle sorting method
US20140346047A1 (en) * 2009-02-17 2014-11-27 Sony Corporation Apparatus and microchip for sorting micro particles
US9145590B2 (en) 2000-05-09 2015-09-29 Xy, Llc Methods and apparatus for high purity X-chromosome bearing and Y-chromosome bearing populations of spermatozoa
AU2013202635B2 (en) * 2013-03-14 2015-10-29 Inguran, Llc Apparatus and methods for high throughput sperm sorting
EP3000874A1 (en) 2014-09-26 2016-03-30 Inguran, LLC Sex sorted sperm demonstrating a dose response and methods of producing sex sorted sperm demonstrating a dose response
WO2016090310A1 (en) 2014-12-05 2016-06-09 Inguran, Llc Cell processing using magnetic particles
US9365822B2 (en) 1997-12-31 2016-06-14 Xy, Llc System and method for sorting cells
US9433195B2 (en) 2012-06-06 2016-09-06 Inguran, Llc Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
US9442059B2 (en) 2011-05-12 2016-09-13 Xy, Llc UV diode laser excitation in flow cytometry
US20170074775A1 (en) * 2014-05-22 2017-03-16 Sony Corporation Particle analyzer
US9879222B2 (en) 2007-12-14 2018-01-30 Mofa Group Llc Gender-specific separation of sperm cells and embryos
US9888990B2 (en) 2012-06-06 2018-02-13 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine
USRE46992E1 (en) 2005-02-01 2018-08-14 Premium Genetics (Uk) Ltd Method and apparatus for sorting cells
USD864415S1 (en) 2018-01-30 2019-10-22 Becton, Dickinson And Company Particle sorting system
USD868991S1 (en) 2017-03-28 2019-12-03 Becton, Dickinson And Company Register block
USD869676S1 (en) 2017-03-28 2019-12-10 Becton, Dickinson And Company Particle sorting module
USD872296S1 (en) 2018-01-30 2020-01-07 Becton, Dickinson And Company Particle sorting module
USD876668S1 (en) 2018-01-30 2020-02-25 Becton, Dickinson And Company Particle sorting module mount
US10620213B2 (en) 2012-10-05 2020-04-14 Inguran, Llc High pressure sperm sorting and flow cytometer methods
USD882817S1 (en) 2018-01-30 2020-04-28 Becton, Dickinson And Company Sample container
WO2020206439A1 (en) * 2019-04-05 2020-10-08 Nanocytomics, LLC Consumable components in fluidic sample dispensing systems and methods
WO2021259903A1 (en) 2020-06-22 2021-12-30 Westfälische Wilhelms-Universität Münster Sperm stratification
US11230695B2 (en) 2002-09-13 2022-01-25 Xy, Llc Sperm cell processing and preservation systems
US11413358B2 (en) 2018-04-09 2022-08-16 Inguran, Llc Sperm nuclei and methods of their manufacture and use
WO2022204600A1 (en) 2021-03-26 2022-09-29 Cytonome/St, Llc Systems and methods for particle sorting with automated adjustment of operational parameters
US11629330B2 (en) 2019-03-19 2023-04-18 Inguran, Llc Method for improved sperm cell populations
US11668640B2 (en) 2015-03-06 2023-06-06 Inguran, Llc Nozzle assembly for a flow cytometry system and methods of manufacture
US12121547B2 (en) 2020-01-20 2024-10-22 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1633259A (zh) * 2000-06-12 2005-06-29 Xy公司 利用分离的带x－染色体和带y－染色体的精子群的综合兽群管理系统
US20020118402A1 (en) * 2000-09-19 2002-08-29 Shaw Timothy C. Film bridge for digital film scanning system
DE102005052752A1 (de) * 2005-11-04 2007-05-10 Clondiag Chip Technologies Gmbh Vorrichtung und Verfahren zum Nachweis von molekularen Wechselwirkungen
US7340957B2 (en) 2004-07-29 2008-03-11 Los Alamos National Security, Llc Ultrasonic analyte concentration and application in flow cytometry
FR2883973B1 (fr) * 2005-03-31 2007-11-16 C2 Diagnostics Sa Cuve pour dispositif optique d'analyse sanguine, appareil d'analyse equipe d'une telle cuve
US20070025879A1 (en) * 2005-07-27 2007-02-01 Dakocytomation Denmark A/S Method and apparatus for syringe-based sample introduction within a flow cytometer
US7618770B2 (en) * 2005-07-29 2009-11-17 Xy, Inc. Methods and apparatus for reducing protein content in sperm cell extenders
US7835000B2 (en) 2006-11-03 2010-11-16 Los Alamos National Security, Llc System and method for measuring particles in a sample stream of a flow cytometer or the like
ATE538377T1 (de) 2007-04-02 2012-01-15 Acoustic Cytometry Systems Inc Verfahren zur verbesserten analyse von in einem akustischen feld fokussierten zellen und partikeln
US7837040B2 (en) * 2007-04-09 2010-11-23 Los Alamos National Security, Llc Acoustic concentration of particles in fluid flow
US8083068B2 (en) 2007-04-09 2011-12-27 Los Alamos National Security, Llc Apparatus for separating particles utilizing engineered acoustic contrast capture particles
US8528406B2 (en) 2007-10-24 2013-09-10 Los Alamos National Security, LLP Method for non-contact particle manipulation and control of particle spacing along an axis
US8263407B2 (en) * 2007-10-24 2012-09-11 Los Alamos National Security, Llc Method for non-contact particle manipulation and control of particle spacing along an axis
US8266950B2 (en) 2007-12-19 2012-09-18 Los Alamos National Security, LLP Particle analysis in an acoustic cytometer
US8714014B2 (en) * 2008-01-16 2014-05-06 Life Technologies Corporation System and method for acoustic focusing hardware and implementations
CA2727478A1 (en) * 2008-06-13 2009-12-17 Xy, Llc Lubricious microfluidic flow path system
WO2011068764A2 (en) * 2009-12-04 2011-06-09 Life Technologies Corporation Apparatuses, systems, methods, and computer readable media for acoustic flow cytometry
US20130011825A1 (en) 2010-04-01 2013-01-10 Inguran, Llc Methods and systems for reducing dna fragmentation in a processed sperm sample
DE102011006080B4 (de) 2011-03-24 2015-06-18 Masterrind Gmbh Vorrichtung und Verfahren zur Fraktionierung von Säugerspermatozoen
DE102011006081A1 (de) 2011-03-24 2012-09-27 Masterrind Gmbh Düse zur Ausrichtung eines Flüssigkeitsteilstroms
DE102011075711A1 (de) 2011-05-12 2012-11-15 Masterrind Gmbh Düse zur Partikelausrichtung im Flüssigkeitsstrom
CN103013811A (zh) * 2011-09-20 2013-04-03 北京富通华投资有限公司 精子分选仪
CN102795668B (zh) * 2012-09-12 2014-07-09 西南大学 一种vo2的制备方法
WO2014047206A1 (en) * 2012-09-18 2014-03-27 Cytonome/St, Llc Flow cell for particle sorting
DE102012108989B3 (de) * 2012-09-24 2014-01-23 Eads Deutschland Gmbh Detektionsvorrichtung sowie Verfahren zur automatischen Detektion von Partikeln
DE202012105015U1 (de) 2012-12-21 2013-03-05 Laser Zentrum Hannover E.V. Einrichtung mit einem inneren und einem äußeren Funktionselement
US9757726B2 (en) 2013-03-14 2017-09-12 Inguran, Llc System for high throughput sperm sorting
US10662408B2 (en) 2013-03-14 2020-05-26 Inguran, Llc Methods for high throughput sperm sorting
US10371622B2 (en) 2013-03-14 2019-08-06 Inguran, Llc Device for high throughput sperm sorting
DE102013208584A1 (de) * 2013-05-08 2014-11-13 Masterrind Gmbh Düse und Verfahren für die Durchflusszytometrie
US10870175B2 (en) * 2013-09-18 2020-12-22 Cytonome/St, Llc Microfluidic flow-through elements and methods of manufacture of same
CN103555662B (zh) * 2013-10-31 2015-09-16 大连金弘基种畜有限公司 将四溴化1,1,2,2-四-[4-(2-三乙基乙氧基胺基)]苯乙烯应用于精子分离
WO2016154131A1 (en) * 2015-03-23 2016-09-29 New York University Systems and methods for selecting cellular strains
WO2017202932A2 (en) 2016-05-24 2017-11-30 Cellix Limited An apparatus for microfluidic flow cytometry analysis of a particulate containing fluid
FR3068469B1 (fr) * 2017-06-28 2020-09-11 Diagdev Cuve de mesure pour le denombrement et/ou la caracterisation de cellules
CN110945343B (zh) 2017-07-19 2023-01-13 英格朗公司 分析仪器和产生精子群体的方法
CN117085750A (zh) * 2018-04-25 2023-11-21 产生技术有限公司 与微流体系统相关联的系统、设备和方法
US20210033521A1 (en) * 2019-07-30 2021-02-04 Diatron MI PLC Flow cytometer and method of analysis
CN111521549B (zh) * 2020-05-13 2021-01-01 洹仪科技(上海)有限公司 一种颗粒分选装置及方法
WO2023186905A1 (en) 2022-03-29 2023-10-05 LAVA Therapeutics N.V. A method of treating a hematological cancer following screening for cd1d positive tumor cells
US20230311134A1 (en) * 2022-03-29 2023-10-05 A. Raymond Et Cie Blended jet spray nozzle
WO2024195948A1 (ko) * 2023-03-22 2024-09-26 엠비디 주식회사 바이오 시료용 고속분주스폿터 및 고속분주스폿터의 세포 분주 방법

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4362246A (en) 1980-07-14 1982-12-07 Adair Edwin Lloyd Method of treating collected mammal semen and separating sperm into X Y components
US4660971A (en) 1984-05-03 1987-04-28 Becton, Dickinson And Company Optical features of flow cytometry apparatus
US4988619A (en) 1987-11-30 1991-01-29 United States Department Of Energy Flow cytometry apparatus
US5135759A (en) 1989-05-10 1992-08-04 The United States Of America As Represented By The Secretary Of Agriculture Method to preselect the sex of offspring
US5371585A (en) 1992-11-10 1994-12-06 Pacific Scientific Company Particle detecting instrument with sapphire detecting cell defining a rectangular flow path
US5439362A (en) 1987-04-08 1995-08-08 Cytogam, Inc. Sex-associated membrane proteins and methods for increasing the probability that offspring will be of a desired sex
US5466572A (en) 1992-09-03 1995-11-14 Systemix, Inc. High speed flow cytometric separation of viable cells
US5483469A (en) 1993-08-02 1996-01-09 The Regents Of The University Of California Multiple sort flow cytometer
WO1996012171A2 (en) 1994-10-14 1996-04-25 University Of Washington High speed flow cytometer droplet formation system
US5602039A (en) 1994-10-14 1997-02-11 The University Of Washington Flow cytometer jet monitor system
US5602349A (en) 1994-10-14 1997-02-11 The University Of Washington Sample introduction system for a flow cytometer
US5690895A (en) 1993-01-26 1997-11-25 Hitachi, Ltd. Flow cell apparatus
US5700692A (en) 1994-09-27 1997-12-23 Becton Dickinson And Company Flow sorter with video-regulated droplet spacing
WO1999005504A2 (en) 1997-07-24 1999-02-04 The United States Of America, As Represented By The Secretary Of Agriculture Flow cytometry nozzle for high efficiency cell sorting

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3661460A (en) * 1970-08-28 1972-05-09 Technicon Instr Method and apparatus for optical analysis of the contents of a sheathed stream
US3893766A (en) * 1973-06-14 1975-07-08 Coulter Electronics Apparatus for orienting generally flat particles for slit-scan photometry
JPS5157484A (en) * 1974-09-20 1976-05-19 Coulter Electronics Ryushihokozukesochi
NO156916C (no) * 1985-07-10 1987-12-16 Harald B Steen Stroemningskammer for vaeskestroemsfotometer.
JPS63262565A (ja) * 1987-04-20 1988-10-28 Hitachi Ltd フロ−セル
JPH0618275Y2 (ja) * 1989-03-09 1994-05-11 東亜医用電子株式会社 フローセル
JP2808321B2 (ja) * 1989-09-19 1998-10-08 東亜医用電子株式会社 細胞分析方法及び装置
JPH0692931B2 (ja) * 1991-03-26 1994-11-16 工業技術院長 液体中繊維状粒子分析計
JP3117751B2 (ja) * 1991-07-26 2000-12-18 シスメックス株式会社 粒子分析用のサンプル扁平流形成装置
JP3075370B2 (ja) * 1991-07-26 2000-08-14 シスメックス株式会社 粒子分析用のサンプル扁平流形成装置
US5311290A (en) * 1992-09-30 1994-05-10 Pulp And Paper Research Institute Of Canada Imaging apparatus and method of fiber analysis
JP3376662B2 (ja) * 1993-01-26 2003-02-10 株式会社日立製作所 フローセル装置
US5601234A (en) * 1994-08-01 1997-02-11 Abbott Laboratories Fluid nozzle and method of introducing a fluid
EP0755576B1 (en) 1994-10-18 2008-03-05 The University Of Southern California Organic fuel cell, and methods of operation thereof and manufacture of electrode therefor
GB9707096D0 (en) * 1997-04-08 1997-05-28 Smithkline Beecham Plc Novel device
US6149867A (en) 1997-12-31 2000-11-21 Xy, Inc. Sheath fluids and collection systems for sex-specific cytometer sorting of sperm
FR2777351B1 (fr) * 1998-04-08 2000-06-23 Hycel Diagnostics Procede et dispositif de mesure de particules en suspension dans un liquide
US6263745B1 (en) 1999-12-03 2001-07-24 Xy, Inc. Flow cytometer nozzle and flow cytometer sample handling methods
US9815403B2 (en) 2016-01-13 2017-11-14 Si-En Technology (Xiamen) Limited LED driver chip for car reading light and state control method thereof

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4362246A (en) 1980-07-14 1982-12-07 Adair Edwin Lloyd Method of treating collected mammal semen and separating sperm into X Y components
US4660971A (en) 1984-05-03 1987-04-28 Becton, Dickinson And Company Optical features of flow cytometry apparatus
US5660997A (en) 1987-04-08 1997-08-26 Cytogam, Inc. Methods for determining antibodies specific for sex associated sperm membrane proteins
US5439362A (en) 1987-04-08 1995-08-08 Cytogam, Inc. Sex-associated membrane proteins and methods for increasing the probability that offspring will be of a desired sex
US4988619A (en) 1987-11-30 1991-01-29 United States Department Of Energy Flow cytometry apparatus
US5135759A (en) 1989-05-10 1992-08-04 The United States Of America As Represented By The Secretary Of Agriculture Method to preselect the sex of offspring
US5466572A (en) 1992-09-03 1995-11-14 Systemix, Inc. High speed flow cytometric separation of viable cells
US5371585A (en) 1992-11-10 1994-12-06 Pacific Scientific Company Particle detecting instrument with sapphire detecting cell defining a rectangular flow path
US5690895A (en) 1993-01-26 1997-11-25 Hitachi, Ltd. Flow cell apparatus
US5483469A (en) 1993-08-02 1996-01-09 The Regents Of The University Of California Multiple sort flow cytometer
US5700692A (en) 1994-09-27 1997-12-23 Becton Dickinson And Company Flow sorter with video-regulated droplet spacing
US5602039A (en) 1994-10-14 1997-02-11 The University Of Washington Flow cytometer jet monitor system
US5602349A (en) 1994-10-14 1997-02-11 The University Of Washington Sample introduction system for a flow cytometer
WO1996012171A2 (en) 1994-10-14 1996-04-25 University Of Washington High speed flow cytometer droplet formation system
US5726364A (en) 1994-10-14 1998-03-10 The University Of Washington Sample introduction apparatus for a flow cytometer
WO1999005504A2 (en) 1997-07-24 1999-02-04 The United States Of America, As Represented By The Secretary Of Agriculture Flow cytometry nozzle for high efficiency cell sorting
US5985216A (en) 1997-07-24 1999-11-16 The United States Of America, As Represented By The Secretary Of Agriculture Flow cytometry nozzle for high efficiency cell sorting

Non-Patent Citations (13)

* Cited by examiner, † Cited by third party
Title
Dean, P. N., Pinkel D. and Mendelsob. n, M. L. 1978. Hydrodynamic orientation of spermatozoa heads for flow cytometry. Biophys. J. 23:7-13.
Fulwyler, M. J. 1977. Hydrodynamic orientation of cells. J Histochem. Cytochem. 25:781-783.
Gurnsey, M. P., and Johnson, L. A., "Recent improvements in efficiency of flow cytometric sorting of X and Y- chromosome bering sperm of domestic animals: a review", 1998, New Zealand Society of Animal Protection, three pages.
Johnson L. A., Flook J.P., Hawk H.W. Sex preseletion in rabbits: Live births from X and Y sperm seperated by DNA and cell sorting. Bio Reprod 41: 199-203, 1989.
Johnson L.A., Flook J.P., Look M.V. 1987. Flow cytometry of X- and Y- chromosome bearing sperm for DNA using an improved preparation method and staining with Hoechst 333-42. Garnete Research 17:203-212.
Johnson L.A., Pinkel D. 1986. Modification of a laser-based flow cytometer for high resolution DNA analysis of mammalian spermatozoa. Cytometry 7:266-273.
Johnson, L.A., Welch, G. R., Garner DL. 1994. Improved flow sorting resolution of X- and Y- chromosome bering viable sperm separation using dual staining and dead cell gating. Cytometry 17 (suppl 7):83.
Johnson, L.A., Welch, G.R., Rens, W. and Dobrinsky, J. R. 1998. Enhanced flow cytometric sorting of manunalian X and Ysperm: high speed sorting and orienting no77.1e for artificial insemination. Theriogenology. 46(1):361. abstr.
Kachel, V., et al., "Uniform Lateral Orientation, Cused by Flow Forces, of Flat Particles in Flow-Through System", The Journal of Histochemistry and Cytochemistry, 1997, vol. 25, No. 7, pp 774-780.
Rens, W., et al., "A Novel Nozzle for More Efficient Sperm Orientation to Improve Sorting Efficiency of X- and Y- Chromosome-Bearing Sperm", Technical Notes, Cytometry 33, 1998, pp 476-481.
Rens, W., et al., "Improved Flow Cytometric Sorting of X-and Y-Chromosome Bearing Sperm: Substantial Increase in Yield of Sexed Semen", Molecular Reproduction and Development, 1999, pp 50-56.
Seidel, G. E. Jr., Herickhoff, L. A., Schenk, J.L., Doyle, S.P. and Green, R.D. 1998. Artifical insemination of heifers with cooled, unfrozen, sexed semen. 1998. Theriogenology. 49(1):365.
Welch G. R., Houck D.W., Johnson L.A., 1994. Fluidic and optical modifications to a FACS IV for flow sorting of X- and Y- chromosome bearing sperm based on DNA. Cytometry 17 (suppl 7): 74.

Cited By (153)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6861265B1 (en) * 1994-10-14 2005-03-01 University Of Washington Flow cytometer droplet formation system
US7923252B2 (en) 1994-10-14 2011-04-12 University Of Washington Droplet formation systems for flow cytometers
US20050153458A1 (en) * 1994-10-14 2005-07-14 University Of Washington Droplet formation systems for flow cytometers
US8553226B2 (en) 1997-01-31 2013-10-08 Xy, Llc Optical apparatus
US20110071035A1 (en) * 1997-01-31 2011-03-24 Xy, Llc Optical Apparatus
US7929137B2 (en) 1997-01-31 2011-04-19 Xy, Llc Optical apparatus
US8975035B2 (en) 1997-01-31 2015-03-10 Xy, Llc Method of analyzing cells
US20110195492A1 (en) * 1997-01-31 2011-08-11 Xy, Llc Optical Apparatus
US9422523B2 (en) 1997-12-31 2016-08-23 Xy, Llc System and method for sorting cells
US9365822B2 (en) 1997-12-31 2016-06-14 Xy, Llc System and method for sorting cells
US7772005B1 (en) 1998-07-30 2010-08-10 Xy, Llc Method of establishing an equine artificial insemination sample
US7820425B2 (en) 1999-11-24 2010-10-26 Xy, Llc Method of cryopreserving selected sperm cells
US6604435B2 (en) 1999-12-03 2003-08-12 Xy, Inc. Low acceleration method of flow cytometry
US6782768B2 (en) 1999-12-03 2004-08-31 Xy, Inc. Flow cytometer nozzle
US20040050186A1 (en) * 1999-12-03 2004-03-18 Xy, Inc. Flow cytometer nozzle
US6357307B2 (en) 1999-12-03 2002-03-19 Xy, Inc. System and method of flow cytometry and sample handling
US10208345B2 (en) 2000-05-09 2019-02-19 Xy, Llc Method for producing high purity X-chromosome bearing and Y-chromosome bearing populations of spermatozoa
US9145590B2 (en) 2000-05-09 2015-09-29 Xy, Llc Methods and apparatus for high purity X-chromosome bearing and Y-chromosome bearing populations of spermatozoa
US7771921B2 (en) 2000-11-29 2010-08-10 Xy, Llc Separation systems of frozen-thawed spermatozoa into X-chromosome bearing and Y-chromosome bearing populations
US8652769B2 (en) 2000-11-29 2014-02-18 Xy, Llc Methods for separating frozen-thawed spermatozoa into X-chromosome bearing and Y-chromosome bearing populations
US8137967B2 (en) 2000-11-29 2012-03-20 Xy, Llc In-vitro fertilization systems with spermatozoa separated into X-chromosome and Y-chromosome bearing populations
US20040132001A1 (en) * 2000-11-29 2004-07-08 Seidel George E System for in-vitro fertilization with spermatozoa separated into x-chromosome and y-chromosome bearing populations
US7713687B2 (en) 2000-11-29 2010-05-11 Xy, Inc. System to separate frozen-thawed spermatozoa into x-chromosome bearing and y-chromosome bearing populations
US9879221B2 (en) 2000-11-29 2018-01-30 Xy, Llc Method of in-vitro fertilization with spermatozoa separated into X-chromosome and Y-chromosome bearing populations
US7012689B2 (en) 2001-05-17 2006-03-14 Dako Colorado, Inc. Flow cytometer with active automated optical alignment system
WO2002092247A1 (en) * 2001-05-17 2002-11-21 Cytomation, Inc. Flow cytometer with active automated optical alignment system
US20040104309A1 (en) * 2002-06-21 2004-06-03 Darko Segota Method and system for regulating external fluid flow over an object's surface, and particularly a wing and diffuser
US20050098685A1 (en) * 2002-06-21 2005-05-12 Darko Segota Method and system for regulating pressure and optimizing fluid flow about a fuselage similar body
US7278825B2 (en) 2002-06-21 2007-10-09 Darko Segota Method and system for regulating fluid over an airfoil or a hydrofoil
US7475853B2 (en) 2002-06-21 2009-01-13 Darko Segota Method and system for regulating external fluid flow over an object's surface, and particularly a wing and diffuser
US20040050064A1 (en) * 2002-06-21 2004-03-18 Darko Segota Method and system for regulating internal fluid flow within an enclosed or semi-enclosed environment
US7296411B2 (en) 2002-06-21 2007-11-20 Darko Segota Method and system for regulating internal fluid flow within an enclosed or semi-enclosed environment
US20050106017A1 (en) * 2002-06-21 2005-05-19 Darko Segota Method and system for regulating fluid over an airfoil or a hydrofoil
US20050106016A1 (en) * 2002-06-21 2005-05-19 Darko Segota Method and system for regulating fluid flow over an airfoil or a hydrofoil
US7048505B2 (en) 2002-06-21 2006-05-23 Darko Segota Method and system for regulating fluid flow over an airfoil or a hydrofoil
US8497063B2 (en) 2002-08-01 2013-07-30 Xy, Llc Sex selected equine embryo production system
US8486618B2 (en) 2002-08-01 2013-07-16 Xy, Llc Heterogeneous inseminate system
US8211629B2 (en) 2002-08-01 2012-07-03 Xy, Llc Low pressure sperm cell separation system
US7855078B2 (en) 2002-08-15 2010-12-21 Xy, Llc High resolution flow cytometer
US11230695B2 (en) 2002-09-13 2022-01-25 Xy, Llc Sperm cell processing and preservation systems
US11261424B2 (en) 2002-09-13 2022-03-01 Xy, Llc Sperm cell processing systems
US7544326B2 (en) 2002-09-27 2009-06-09 Becton, Dickinson And Company Fixed mounted sorting cuvette with user replaceable nozzle
US20080291425A1 (en) * 2002-09-27 2008-11-27 Norton Pierce O Removable sorting cuvette and nozzle
US20040062685A1 (en) * 2002-09-27 2004-04-01 Norton Pierce O Fixed mounted sorting cuvette with user replaceable nozzle
US7201875B2 (en) 2002-09-27 2007-04-10 Becton Dickinson And Company Fixed mounted sorting cuvette with user replaceable nozzle
US20050072677A1 (en) * 2003-02-18 2005-04-07 Board Of Regents, The University Of Texas System Dielectric particle focusing
US8617904B2 (en) 2003-03-28 2013-12-31 Inguran, Llc Sperm cell processing methods
US11718826B2 (en) 2003-03-28 2023-08-08 Inguran, Llc System and method for sorting particles
US7335507B2 (en) 2003-03-28 2008-02-26 Monsanto Technology Llc Process for the staining of sperm
EP2308418A2 (en) 2003-03-28 2011-04-13 Inguran, LLC Apparatus and methods for providing sex-sorted animal sperm
EP2306174A2 (en) 2003-03-28 2011-04-06 Inguran, LLC Apparatus and methods for providing sex-sorted animal sperm
US7943384B2 (en) 2003-03-28 2011-05-17 Inguran Llc Apparatus and methods for sorting particles
US10100278B2 (en) 2003-03-28 2018-10-16 Inguran, Llc Multi-channel system and methods for sorting particles
US20050003472A1 (en) * 2003-03-28 2005-01-06 Monsanto Technology Llc Process for the staining of sperm
US20110215111A1 (en) * 2003-03-28 2011-09-08 Inguran, Llc Method and apparatus for orienting sperm in a fluid stream
US20110217723A1 (en) * 2003-03-28 2011-09-08 Inguran, Llc Epi-illumination apparatus and methods for sorting particles
US20110217722A1 (en) * 2003-03-28 2011-09-08 Inguran, Llc Photo-damage apparatus and methods for sorting particles
US8748183B2 (en) 2003-03-28 2014-06-10 Inguran, Llc Method and apparatus for calibrating a flow cytometer
EP2306174A3 (en) * 2003-03-28 2012-01-04 Inguran, LLC Apparatus and methods for providing sex-sorted animal sperm
EP2308418A3 (en) * 2003-03-28 2012-01-04 Inguran, LLC Apparatus and methods for providing sex-sorted animal sperm
US7799569B2 (en) 2003-03-28 2010-09-21 Inguran, Llc Process for evaluating staining conditions of cells for sorting
US8198093B2 (en) 2003-03-28 2012-06-12 Inguran Llc Methods for sorting particles
US8198092B2 (en) 2003-03-28 2012-06-12 Inguran, Llc Digital sampling apparatus and methods for sorting particles
US8206987B2 (en) * 2003-03-28 2012-06-26 Inguran Llc Photo-damage method for sorting particles
US8206988B2 (en) * 2003-03-28 2012-06-26 Inguran Llc Method and apparatus for orienting sperm in a fluid stream
US7758811B2 (en) 2003-03-28 2010-07-20 Inguran, Llc System for analyzing particles using multiple flow cytometry units
US8709825B2 (en) * 2003-03-28 2014-04-29 Inguran, Llc Flow cytometer method and apparatus
US8241914B2 (en) * 2003-03-28 2012-08-14 Inguran Llc EPI-damage apparatus and methods for sorting particles
AU2012200711B2 (en) * 2003-03-28 2012-09-20 Inguran, Llc "Method and apparatus for orientating sperm in a fluid stream"
WO2004088283A3 (en) * 2003-03-28 2005-08-11 Monsanto Technology Llc Apparatus and methods for providing sex-sorted animal sperm
US8709817B2 (en) 2003-03-28 2014-04-29 Inguran, Llc Systems and methods for sorting particles
WO2004088283A2 (en) * 2003-03-28 2004-10-14 Monsanto Technology Llc Apparatus and methods for providing sex-sorted animal sperm
US20130224787A1 (en) * 2003-03-28 2013-08-29 Inguran, Llc Flow cytometer method and apparatus
US8535938B2 (en) 2003-03-28 2013-09-17 Inguran, Llc Photo-damage apparatus for sorting particles
US11104880B2 (en) 2003-03-28 2021-08-31 Inguran, Llc Photo-damage system for sorting particles
US8609422B2 (en) 2003-03-28 2013-12-17 Inguran, Llc Method and apparatus for sorting particles
US9377390B2 (en) 2003-03-28 2016-06-28 Inguran, Llc Apparatus, methods and processes for sorting particles and for providing sex-sorted animal sperm
US8623657B2 (en) 2003-03-28 2014-01-07 Inguran, Llc Flow cytometer apparatus and method
US8623658B2 (en) 2003-03-28 2014-01-07 Inguran, Llc Methods for processing sperm cells
US8637318B2 (en) 2003-03-28 2014-01-28 Inguran, Llc Methods for sorting particles
US8691584B2 (en) 2003-03-28 2014-04-08 Inguran, Llc Sperm processing methods
US8664006B2 (en) * 2003-03-28 2014-03-04 Inguran, Llc Flow cytometer apparatus and method
US9040304B2 (en) 2003-03-28 2015-05-26 Inguran, Llc Multi-channel system and methods for sorting particles
US7723116B2 (en) 2003-05-15 2010-05-25 Xy, Inc. Apparatus, methods and processes for sorting particles and for providing sex-sorted animal sperm
US20080153087A1 (en) * 2004-02-05 2008-06-26 Select Xy Limited Method and Apparatus For Orienting Aspherical Cells
US20050282245A1 (en) * 2004-03-29 2005-12-22 Monsanto Technology Llc Use of a composition which regulates oxidation/reduction reactions intracellularly and/or extracellularly in a staining or sorting process
EP2151243A2 (en) 2004-03-29 2010-02-10 Inguran, LLC Sperm suspensions for sorting into X or Y chromosome-bearing enriched populations
US20050244805A1 (en) * 2004-03-29 2005-11-03 Monsanto Technology Llc Sperm suspensions for sorting into X or Y chromosome-bearing enriched populations
US20050214733A1 (en) * 2004-03-29 2005-09-29 Monsanto Technology Llc Sperm suspensions for use in insemination
US7998700B2 (en) 2004-03-29 2011-08-16 Inguran, Llc Use of a composition which regulates oxidation/reduction reactions intracellularly and/or extracellulary in a staining or sorting process
EP2801363A1 (en) 2004-03-29 2014-11-12 Inguran, LLC Sperm suspensions for use in insemination
US7838210B2 (en) 2004-03-29 2010-11-23 Inguran, LLC. Sperm suspensions for sorting into X or Y chromosome-bearing enriched populations
US7833147B2 (en) 2004-07-22 2010-11-16 Inguran, LLC. Process for enriching a population of sperm cells
USRE46992E1 (en) 2005-02-01 2018-08-14 Premium Genetics (Uk) Ltd Method and apparatus for sorting cells
US9879222B2 (en) 2007-12-14 2018-01-30 Mofa Group Llc Gender-specific separation of sperm cells and embryos
US20090283148A1 (en) * 2008-05-13 2009-11-19 Sony Corporation Microchip and channel structure for the same
US9861984B2 (en) 2008-05-13 2018-01-09 Sony Corporation Microchip and channel structure for the same
US9409172B2 (en) 2008-05-13 2016-08-09 Sony Corporation Microchip and channel structure for the same
US20100009333A1 (en) * 2008-07-08 2010-01-14 Beckman Coulter, Inc. Methods for Acoustic Particle Focusing in Biological Sample Analyzers
DE102008033570A1 (de) * 2008-07-15 2010-02-11 Masterrind Gmbh Verfahren zur Zellidentifikation und Zellsortierung
DE102008033570B4 (de) * 2008-07-15 2010-09-30 Masterrind Gmbh Verfahren zur Zellidentifikation und Zellsortierung
US20140346047A1 (en) * 2009-02-17 2014-11-27 Sony Corporation Apparatus and microchip for sorting micro particles
USRE50088E1 (en) 2009-02-17 2024-08-20 Sony Corporation Microchip for sorting micro particles and cartridge including same
US9588036B2 (en) 2009-02-17 2017-03-07 Sony Corporation Microchip for sorting micro particles and cartridge including same
US9207160B2 (en) * 2009-02-17 2015-12-08 Sony Corporation Apparatus and microchip for sorting micro particles
USRE48827E1 (en) 2009-02-17 2021-11-23 Sony Corporation Microchip for sorting micro particles and cartridge including same
US20110236923A1 (en) * 2010-03-23 2011-09-29 Genetics & Ivf Institute Method for staining and sorting of a small volume of sperm
WO2012106294A1 (en) 2011-02-04 2012-08-09 Cytonome/St, Llc Particle sorting apparatus and method
EP3913354A1 (en) 2011-05-12 2021-11-24 Xy, Llc Uv diode laser excitation in flow cytometry
US9442059B2 (en) 2011-05-12 2016-09-13 Xy, Llc UV diode laser excitation in flow cytometry
US20130020498A1 (en) * 2011-07-19 2013-01-24 Sysmex Corporation Flow cytometer
US9433195B2 (en) 2012-06-06 2016-09-06 Inguran, Llc Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
US10219883B2 (en) 2012-06-06 2019-03-05 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine
US10543070B2 (en) 2012-06-06 2020-01-28 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine
US10542734B2 (en) 2012-06-06 2020-01-28 Inguran, Llc Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
US9888990B2 (en) 2012-06-06 2018-02-13 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine
US10188082B2 (en) 2012-06-06 2019-01-29 Inguran, Llc Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
US11653635B2 (en) 2012-06-06 2023-05-23 Inguran, Llc Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
US9222872B2 (en) 2012-09-19 2015-12-29 Inguran, Llc Flow cytometer nozzle tip
US9404846B2 (en) 2012-09-19 2016-08-02 Inguran, Llc Nozzle assembly for a flow cytometer system and methods of manufacture
US9927345B2 (en) 2012-09-19 2018-03-27 Inguran, Llc Nozzle assembly for a flow cytometer
US9027850B2 (en) 2012-09-19 2015-05-12 Inguran, Llc Nozzle assembly for a flow cytometer system and methods of manufacture
WO2014046733A1 (en) 2012-09-19 2014-03-27 Inguran, Llc Nozzle assembly for a flow cytometer system and methods of manufacture
US10634601B2 (en) 2012-09-19 2020-04-28 Inguran, Llc Nozzle assembly for a flow cytometry system and methods of manufacture
WO2014047358A1 (en) 2012-09-19 2014-03-27 Inguran, Llc Flow cytometer nozzle tip
EP4163618A1 (en) 2012-09-19 2023-04-12 Inguran, LLC A method of manufacturing a flow cytometer nozzle assembly
EP4230996A2 (en) 2012-09-19 2023-08-23 Inguran, LLC A method of sorting cells and a flow cytometer system
US10620213B2 (en) 2012-10-05 2020-04-14 Inguran, Llc High pressure sperm sorting and flow cytometer methods
US11448653B2 (en) 2012-10-05 2022-09-20 Inguran, Llc High pressure sperm sorting and flow cytometer methods
WO2014055773A2 (en) 2012-10-05 2014-04-10 Inguran, Llc High pressure sperm sorting and flow cytometer methods
WO2014055112A1 (en) 2012-10-05 2014-04-10 Inguran, Llc High efficiency methods of sex sorting sperm
US10400213B2 (en) 2012-10-05 2019-09-03 Inguran, Llc High efficiency methods of sex sorting sperm
US9429276B2 (en) * 2013-03-13 2016-08-30 Sony Corporation Flow channel device, particle sorting apparatus, particle outflow method, and particle sorting method
US20140261757A1 (en) * 2013-03-13 2014-09-18 Sony Corporation Flow channel device, particle sorting apparatus, particle outflow method, and particle sorting method
AU2013202635B2 (en) * 2013-03-14 2015-10-29 Inguran, Llc Apparatus and methods for high throughput sperm sorting
US10006849B2 (en) * 2014-05-22 2018-06-26 Sony Corporation Particle analyzer
US20170074775A1 (en) * 2014-05-22 2017-03-16 Sony Corporation Particle analyzer
EP3000874A1 (en) 2014-09-26 2016-03-30 Inguran, LLC Sex sorted sperm demonstrating a dose response and methods of producing sex sorted sperm demonstrating a dose response
WO2016090310A1 (en) 2014-12-05 2016-06-09 Inguran, Llc Cell processing using magnetic particles
US11668640B2 (en) 2015-03-06 2023-06-06 Inguran, Llc Nozzle assembly for a flow cytometry system and methods of manufacture
USD869676S1 (en) 2017-03-28 2019-12-10 Becton, Dickinson And Company Particle sorting module
USD868991S1 (en) 2017-03-28 2019-12-03 Becton, Dickinson And Company Register block
USD872296S1 (en) 2018-01-30 2020-01-07 Becton, Dickinson And Company Particle sorting module
USD882817S1 (en) 2018-01-30 2020-04-28 Becton, Dickinson And Company Sample container
USD876668S1 (en) 2018-01-30 2020-02-25 Becton, Dickinson And Company Particle sorting module mount
USD864415S1 (en) 2018-01-30 2019-10-22 Becton, Dickinson And Company Particle sorting system
US11413358B2 (en) 2018-04-09 2022-08-16 Inguran, Llc Sperm nuclei and methods of their manufacture and use
US11629330B2 (en) 2019-03-19 2023-04-18 Inguran, Llc Method for improved sperm cell populations
WO2020206439A1 (en) * 2019-04-05 2020-10-08 Nanocytomics, LLC Consumable components in fluidic sample dispensing systems and methods
US12121547B2 (en) 2020-01-20 2024-10-22 Inguran, Llc Methods for use of sex sorted semen to improve genetic management in swine
WO2021259903A1 (en) 2020-06-22 2021-12-30 Westfälische Wilhelms-Universität Münster Sperm stratification
WO2022204600A1 (en) 2021-03-26 2022-09-29 Cytonome/St, Llc Systems and methods for particle sorting with automated adjustment of operational parameters
US11858008B2 (en) 2021-03-26 2024-01-02 Cytonome/St, Llc Systems and methods for particle sorting with automated adjustment of operational parameters

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